A role for macromolecular crowding effects in the assembly and function of compartments in the nucleus

被引:128
作者
Hancock, R [1 ]
机构
[1] Univ Laval, Ctr Canc Res, Hotel Dieu Hosp, Quebec City, PQ G1R 2J6, Canada
基金
加拿大健康研究院;
关键词
nuclear compartments; nucleolus; PML body; macromolecular crowding;
D O I
10.1016/j.jsb.2003.12.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mechanisms which cause macromolecules to form discrete compartments within the nucleus are not understood. Here, two ubiquitous compartments, nucleoli, and PML bodies, are shown to disassemble when K562 cell nuclei expand in medium of low monovalent cation concentration; their major proteins dispersed as seen by immunofluorescence and immunoelectron microscopy, and nucleolar transcript elongation fell by similar to85%. These compartments reassembled and nucleolar transcription recovered in the same medium after adding inert, penetrating macromolecules (8 kDa polyethylene glycol (PEG), or 10.5 kDa dextran) to 12% w/v, showing that disassembly was not caused by the low cation concentration. These responses satisfy the criteria for crowding or volume exclusion effects which occur in concentrated mixtures of macromolecules; upon expansion the macromolecular concentration within the nucleus falls, and can be restored by PEG or dextran. These observations, together with evidence of a high concentration of macromolecules in the nucleus (in the range of 100mg/ml) which must cause strong crowding forces, suggest strongly that these forces play an essential role in driving the formation, and maintaining the function of nuclear compartments. This view is consistent with their dynamic and mobile nature and can provide interpretations of several unexplained observations in nuclear biology. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:281 / 290
页数:10
相关论文
共 69 条
[1]  
ADAM SA, 1992, METHOD ENZYMOL, V219, P97
[2]  
Andersen JS, 2002, CURR BIOL, V12, P1, DOI 10.1016/S0960-9822(01)00650-9
[3]  
Biggiogera M, 2001, J CELL SCI, V114, P3199
[4]   CONCENTRATION EVALUATION OF CHROMATIN IN UNSTAINED RESIN-EMBEDDED SECTIONS BY MEANS OF LOW-DOSE RATIO-CONTRAST IMAGING IN STEM [J].
BOHRMANN, B ;
HAIDER, M ;
KELLENBERGER, E .
ULTRAMICROSCOPY, 1993, 49 (1-4) :235-251
[5]   The transcription coactivator CBP is a dynamic component of the promyelocytic leukemia nuclear body [J].
Boisvert, FM ;
Kruhlak, MJ ;
Box, AK ;
Hendzel, MJ ;
Bazett-Jones, DP .
JOURNAL OF CELL BIOLOGY, 2001, 152 (05) :1099-1106
[6]  
Busch H, 1977, Methods Cell Biol, V16, P1
[7]   Reevaluation of transcriptional regulation by TATA-binding protein oligomerization: Predominance of monomers [J].
Campbell, KM ;
Ranallo, RT ;
Stargell, LA ;
Lumb, KJ .
BIOCHEMISTRY, 2000, 39 (10) :2633-2638
[8]   Macromolecular mobility inside the cell nucleus [J].
Carmo-Fonseca, M ;
Platani, M ;
Swedlow, JR .
TRENDS IN CELL BIOLOGY, 2002, 12 (11) :491-495
[9]   THE PML GENE ENCODES A PHOSPHOPROTEIN ASSOCIATED WITH THE NUCLEAR MATRIX [J].
CHANG, KS ;
FAN, YH ;
ANDREEFF, M ;
LIU, JX ;
MU, ZM .
BLOOD, 1995, 85 (12) :3646-3653
[10]   Nucleolar components involved in ribosome biogenesis cycle between the nucleolus and nucleoplasm in interphase cells [J].
Chen, DY ;
Huang, S .
JOURNAL OF CELL BIOLOGY, 2001, 153 (01) :169-176